Heavy chain constant regions with reduced binding to Fc gamma receptors

US12509516B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12509516-B2
Application numberUS-202217961442-A
CountryUS
Kind codeB2
Filing dateOct 6, 2022
Priority dateMar 30, 2015
Publication dateDec 30, 2025
Grant dateDec 30, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides antibody heavy chain constant regions with a hinge region modified to reduce binding to Fcγ receptors. The modification occurs within positions 233-236 by replacement of natural residues by glycine(s) and/or deletion(s). Such modifications can reduce binding of an antibody bearing such a constant region to Fcγ receptors to background levels. The constant regions can be incorporated into any format of antibody or Fc fusion protein. Such antibodies or fusion proteins can be used in methods of treatment, particularly those in which the mechanisms of action of the antibody or Fc fusion protein is not primarily or at all dependent on effector functions, as is the case when an antibody inhibits a receptor-ligand interaction or agonizes a receptor.

First claim

Opening claim text (preview).

What is claimed is: 1 . A bispecific antibody comprising: a first heavy chain duplexed with a light chain, wherein the heavy chain comprises a heavy chain variable region and a heavy chain constant region that is human IgG1, IgG2, or IgG4 isotype, wherein amino acid positions 233-236 of a hinge domain are G, G, G and unoccupied; G, G, unoccupied, and unoccupied; G, unoccupied, unoccupied, and unoccupied; or all unoccupied, with amino acid positions numbered by EU numbering, and the light chain comprises a light chain variable region and a light chain constant region, and wherein the heavy chain variable region and the light chain variable region form a first antigen-binding domain that binds a target antigen; and a second heavy chain duplexed with a light chain, wherein the heavy chain comprises a heavy chain variable region and a heavy chain constant region that is human IgG1, IgG2, or IgG4 isotype, wherein amino acid positions 233-236 of a hinge domain are G, G, G and unoccupied; G, G, unoccupied, and unoccupied; G, unoccupied, unoccupied, and unoccupied; or all unoccupied, with amino acid positions numbered by EU numbering, and the light chain comprises a light chain variable region and a light chain constant region, and wherein the heavy chain variable region and the light chain variable region form a second antigen-binding domain that binds an antigen on an effector cell. 2 . The bispecific antibody of claim 1 , wherein the target antigen is an antigen on a cancer cell. 3 . The bispecific antibody of claim 1 , wherein the target antigen is an antigen on a pathogen. 4 . The bispecific antibody of claim 1 , wherein the antigen on the effector cell is CD3. 5 . The bispecific antibody of claim 1 , wherein the first heavy chain the second heavy chain are of isotype IgG4. 6 . The bispecific antibody of claim 5 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 5, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 9; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 9, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 5. 7 . The bispecific antibody of claim 5 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 6, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 10; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 10, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 6. 8 . The bispecific antibody of claim 5 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 7, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 11; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 11, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 7. 9 . The bispecific antibody of claim 5 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 8, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 12; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 12, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 8. 10 . The bispecific antibody of claim 1 , wherein the first heavy chain the second heavy chain are of isotype IgG1. 11 . The bispecific antibody of claim 10 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 16, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 20; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 20, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 16. 12 . The bispecific antibody of claim 10 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 17, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 21; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 21, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 17. 13 . The bispecific antibody of claim 10 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 18, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 22; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 22, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 18. 14 . The bispecific antibody of claim 10 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 19, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 23; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 23, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 19. 15 . The bispecific antibody of claim 1 , wherein the first heavy chain the second heavy chain are of isotype IgG2. 16 . The bispecific antibody of claim 15 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 24, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 28; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 28, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 24. 17 . The bispecific antibody of claim 15 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 25, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 29; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 29, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 25. 18 . The bispecific antibody of claim 15 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 26, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 30; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 30, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 26. 19 . The bispecific antibody of claim 15 , wherein: the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 27, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 31; or the first heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 31, and the second heavy chain comprises a heavy chain constant region comprising SEQ ID NO: 27.

Assignees

Inventors

Classifications

  • Antibody-dependent cellular cytotoxicity [ADCC] · CPC title

  • CH3 domain · CPC title

  • characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin · CPC title

  • against the immunoglobulin superfamily · CPC title

  • containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered · CPC title

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What does patent US12509516B2 cover?
The invention provides antibody heavy chain constant regions with a hinge region modified to reduce binding to Fcγ receptors. The modification occurs within positions 233-236 by replacement of natural residues by glycine(s) and/or deletion(s). Such modifications can reduce binding of an antibody bearing such a constant region to Fcγ receptors to background levels. The constant regions can be in…
Who is the assignee on this patent?
Regeneron Pharma
What technology area does this patent fall under?
Primary CPC classification C07K16/2803. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).